Prevalence of mitochondrial gene mutations in families with diabetes mellitus
- 4 December 1993
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 342 (8884), 1429-1430
- https://doi.org/10.1016/0140-6736(93)92792-r
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Japanese case of diabetes mellitus and . deafness with mutation in mitochondrial tRNALeu(UUR)geneThe Lancet, 1993
- Familial Hyperglycemia Due to Mutations in Glucokinase -- Definition of a Subtype of Diabetes MellitusNew England Journal of Medicine, 1993
- Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNAThe Lancet, 1992
- Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafnessNature Genetics, 1992